The aim of this work was to synthesise a series of three ferrocene derivatives bearing either amine, amide or hydrazine groups and to evaluate their in vitro antioxidant activities. Spectrophotometrical and electrochemical techniques were used to quantify the total antioxidant activities, the former was carried out using 1,1-diphenyl-2- picrylhydrazyl and phosphomolybdenum reagents, the latter was based on measuring the oxidation peak current of superoxide anion radical electrochemically generated by reduction of commercial molecular oxygen in DMSO. The ferrocenic derivative N’-ferrocenylmethyl-N’-phenylbenzohydrazide shows the highest DPPH and .radicals scavenging activities (0.1 ± 0.00245) and (0.92 ± 0.04 mg/ml) respectively which was significantly closer to that of standard antioxidant ascorbic acid. The results of both spectrophotometrical and electrochemical tests indicate that the activity depends strongly upon the presence of a nitrogen atom in the molecule but is improved by the influence of the hydrazine function. In addition spectrophotometrical tests of N-(Ferrocenylmethyl)-2-nitrobenzenamine does not give any activity due to its deep purple colour, however the antioxidant activity of this derivative was easily measured using electrochemical tests.